FDA 510(k)
FDA class 1
Substantially Equivalent
🇮🇱 Israel
LARYNGOSCOPE BLADES
K Number: K883414
·
Decision Aug 19, 1988
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
63
Applicant Total
4
Review Days
4
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Basic Information
- Device Name
- LARYNGOSCOPE BLADES
- K Number
- K883414
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5540
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Truphatek, Ltd.
- Date Received
- August 15, 1988
- Decision Date
- August 19, 1988
- Product Code
- CCW
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| CCW | Laryngoscope, Rigid | FDA class 1 | Anesthesiology |
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